Author

T. Yoshizawa

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Biochemistry· 3

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:cell type annotation· 2 Assay:bulk RNA-seq· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:chromatin & epigenetic regulation· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1

Frequent Co-Authors

E. Mori· 1 shared E. Ono· 1 shared H. Kajiura· 1 shared H. Koga· 1 shared H. Kumeta· 1 shared H. Matsumura· 1 shared H. Nanaura· 1 shared I. Ota· 1 shared

Activity by Year

2022-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 18 mutual co-author links

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1 shared paperBiochemistry

E. Mori

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Zinc finger domains bind low-complexity domain polymers

N. Iguchi, N. Isozumi, Y. Hattori, T. Imamura, M. So, H. Nanaura, T. Kiriyama, N. Eura, M. Yamaoka, M. Nakanishi, M. Mori, S. Ohki, H. Kumeta, H. Koga, M. Watabe, , E. Mori

This study shows zinc finger domains bind low-complexity domain polymers in a cross-β-dependent manner, suppressing polymer formation and preferentially recognizing polymeric LC domains.

bioRxiv · Oct 29, 2023 · PreprintBiochemistry

Discovery of the apiosyltransferase, celery UGT94AX1 that catalyzes the biosynthesis of a flavone glycoside, apiin

M. Yamashita, T. Fujimori, S. An, S. Iguchi, Y. Takenaka, H. Kajiura, T. Yoshizawa, H. Matsumura, M. Kobayashi, E. Ono, T. Ishimizu

This paper identifies celery UGT94AX1 as the apiosyltransferase responsible for apiin biosynthesis and characterizes its substrate specificity and key residues.

bioRxiv · May 22, 2023 · PreprintBiochemistry

Hypoxia causes pancreatic β-cell dysfunction by activating a transcriptional repressor BHLHE40

T. Tsuyama, Y. Sato, T. Yoshizawa, T. Matsuoka, K. Yamagata

This study identifies BHLHE40 as a hypoxia-induced transcriptional repressor that suppresses insulin secretion in pancreatic β-cells, contributing to β-cell dysfunction in type 2 diabetes.

bioRxiv · Jun 28, 2022 · PreprintBiochemistry